Variation in the 3-Hydroxyl-3-Methylglutaryl Coenzyme A Reductase Gene Is Associated With Racial Differences in Low-Density Lipoprotein Cholesterol Response to Simvastatin Treatment

Author:

Krauss Ronald M.1,Mangravite Lara M.1,Smith Joshua D.1,Medina Marisa W.1,Wang Dai1,Guo Xiuqing1,Rieder Mark J.1,Simon Joel A.1,Hulley Steven B.1,Waters David1,Saad Mohammed1,Williams Paul T.1,Taylor Kent D.1,Yang Huiying1,Nickerson Deborah A.1,Rotter Jerome I.1

Affiliation:

1. From the Children’s Hospital of Oakland Research Institute, Oakland, Calif (R.M.K., L.M.M., M.W.M.); Department of Genome Sciences, University of Washington, Seattle (J.D.S., M.J.R., D.A.N.); Medical Genetics Institute, Cedars-Sinai Medical Center (D. Wang, X.G., K.D.T., H.Y., J.I.R.), and Departments of Medicine and Pediatrics, University of California, Los Angeles, School of Medicine (X.G., K.D.T., H.Y., J.I.R.), Los Angeles; General Internal Medicine Section, Medical Service, Veterans Affairs...

Abstract

Background— Use of 3-hydroxyl-3-methylglutaryl-3 coenzyme A reductase (HMGCR) inhibitors, or statins, reduces cardiovascular disease risk by lowering plasma low-density lipoprotein cholesterol (LDL-C) concentrations. However, LDL-C response is variable and influenced by many factors, including racial ancestry, with attenuated response in blacks compared with whites. We hypothesized that single nucleotide polymorphisms in the gene encoding HMGCR , a rate-limiting enzyme in cholesterol synthesis and the direct enzymatic target of statins, contribute to variation in statin response. Methods and Results— Genomic resequencing of HMGCR in 24 blacks and 23 whites identified 79 single nucleotide polymorphisms. Eleven single nucleotide polymorphisms were selected to tag common linkage disequilibrium clusters. These single nucleotide polymorphisms and the common haplotypes inferred from them were tested for association with plasma LDL-C and LDL-C response to simvastatin treatment (40 mg/d for 6 weeks) in 326 blacks and 596 whites. Black carriers of H7 and/or H2 had significantly lower baseline LDL-C ( P =0.0006) and significantly attenuated LDL-C response compared with black participants who did not carry either haplotype as measured by absolute response (−1.23±0.04 mmol/L, n=209, versus −1.45±0.06 mmol/L, n=117; P =0.0008) and percent response (−36.9±1.0% versus −40.6±1.3%; P =0.02), but no haplotype effect was observed in whites. Percent LDL-C response was lowest in carriers of both H2 and H7, all but one of whom were black (−28.2±4.9%, n=12 H2+H7 carriers, versus −41.5±0.5%, n=650 H2/H7 noncarriers; P =0.001). LDL-C responses in H7 and/or H2 noncarriers were indistinguishable between blacks and whites. Conclusions— HMGCR gene polymorphisms are associated with reduced plasma LDL-C and LDL-C response to simvastatin, and these effects are most evident in blacks.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Cited by 141 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3